Emx1-specific expression of foreign genes using "knock-in" approach

被引:37
作者
Jin, XL
Guo, HL
Mao, CJ
Atkins, N
Wang, H
Avasthi, PP
Tu, YT
Li, YQ [1 ]
机构
[1] Univ Illinois, Dept Mol & Integrat Physiol, Neurosci Program, Urbana, IL 61801 USA
[2] Univ Illinois, Beckman Inst Adv Sci & Technol, Urbana, IL 61801 USA
关键词
cerebral cortex; hippocampus; olfactory bulbs; amygdala; Cre/loxP; transgenic mice; Emx1; beta-galactosidase; knock-in; developing limbs;
D O I
10.1006/bbrc.2000.2532
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
Emx1 is a mouse homologue of the Drosophila homeobox gene empty spiracles. Its expression is limited to the neurons in developing and adult cerebral cortex and hippocampus. Because of the highly restricted expression pattern of the Emx1 gene, it would be quite desirable to characterize the promoter of the Emx1 for directing foreign gene expression in the transgenic mouse, We report here that me have achieved the Emx1-specific expression in transgenic mice by inserting the lacZ reporter and cre genes directly into the exon 1 of the Emx1 gene using embryonic stem (ES) cell technology. The distribution of the beta-galactosidase activity in the transgenic mice was consistent with the published results obtained using in situ hybridization and immunohistochemistry. Furthermore, we have demonstrated that Cre protein was present in the cerebral cortex of the transgenic mice and was able to mediate loxP-specific recombination in vitro, The creation of this line of cre transgenic mice, and the demonstration that the insertion site located in the exon 1 of the Emx1 gene could render foreign genes a specific expression pattern restricted to the developing and adult cerebral cortex and hippocampus, should be conducive to further studies of the effect of a gene mutation or overexpression upon the development and plasticity of cerebral cortex and hippocampus. (C) 2000 Academic Press.
引用
收藏
页码:978 / 982
页数:5
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